Evidence map›Paper›PMID 30980316›Full record

ArticleLifetime data analysis2020

Assessing the value of a censored surrogate outcome.

Layla Parast, Lu Tian, Tianxi Cai

Abstract read
In one paragraph

Article in Lifetime data analysis, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Trial
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Layla ParastStatistics Group, RAND Corporation, 1776 Main Street, Santa Monica, CA, 90266, USA. parast@rand.org.ORCID 0000-0002-7288-1009
Lu TianDepartment of Biomedical Data Science, Stanford University, 365 Lasuen Street, Littlefield Center MC 2069, Stanford, CA, 94305, USA.
Tianxi CaiDepartment of Biostatistics, Harvard T.H. Chan School of Public Health, 665 Huntington Avenue Building 2, Room 405, Boston, MA, 02115, USA.

Funding

TrainingU54HG007963 · NHGRI · HARVARD MEDICAL SCHOOL · PI KOHANE, ISAAC S., MURPHY, SHAWN N · 2014 to 2018
$18.3M
Robust Statistical Methods to Identify and Use Surrogate Markers in DiabetesR01DK118354 · NIDDK · UNIVERSITY OF TEXAS AT AUSTIN · PI PARAST, LAYLA · 2018 to 2025
$2.0M
Robust Statistical Methods to Identify Surrogate Markers in DiabetesR21DK103118 · NIDDK · RAND CORPORATION · PI PARAST, LAYLA · 2014 to 2015
$476k
NHGRI NIH HHS U54 HG007963NIDDK NIH HHS R01 DK118354NIDDK NIH HHS R21 DK103118
6 · The paper itself

Abstract

Assessing the potential of surrogate markers and surrogate outcomes for replacing a long term outcome is an active area of research. The interest in this topic is partly motivated by increasing pressure from stakeholders to shorten the time required to evaluate the safety and/or efficacy of a treatment or intervention such that treatments deemed safe and effective can be made available to those in need more quickly. Most existing methods in surrogacy evaluation either require strict model assumptions or that primary outcome and surrogate outcome information is available for all study participants. In this paper, we focus on a setting where the primary outcome is subject to censoring and the aim is to quantify the surrogacy of an intermediate outcome, which is also subject to censoring. We define the surrogacy as the proportion of treatment effect on the primary outcome that is explained by the intermediate surrogate outcome information and propose two robust methods to estimate this quantity. We propose both a nonparametric approach that uses a kernel smoothed Nelson-Aalen estimator of conditional survival, and a semiparametric method that derives conditional survival estimates from a landmark Cox proportional hazards model. Simulation studies demonstrate that both approaches perform well in finite samples. Our methodological development is motivated by our interest in investigating the use of a composite cardiovascular endpoint as a surrogate outcome in a randomized study of the effectiveness of angiotensin-converting enzyme inhibitors on survival. We apply the proposed methods to quantify the surrogacy of this potential surrogate outcome for the primary outcome, time to death.

Indexed as

BiomarkersOutcome Assessment, Health CareAlgorithmsHumansModels, StatisticalProportional Hazards ModelsSurvival AnalysisBiomarkersKernelNonparametricSurrogateSurvival analysis

Identifiers

PMID30980316
PMCPMC6790145

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.